Literature DB >> 4000268

Position-dependent properties of retinal axons and their growth cones.

F Bonhoeffer, J Huf.   

Abstract

The formation of the very orderly neuronal projection from the retina to the optic tectum is not yet understood, but several mechanisms are thought to be involved in a coordinated fashion. These mechanisms may include mechanical or chemical guidance in channels, guidance by spatial gradients of positional markers, gradients of temporal (maturation) markers or specific inter-axon interactions (see ref. 1 for review). The last-mentioned mechanism could explain the fibre order found in optic nerve and tract. It requires that some or all growing retinal axons can distinguish between retinal axons of various origins and grow preferentially along retinal axons originating from the same area as themselves. The in vitro experiments described here show that growth cones from the temporal half of the chick retina grow preferentially along temporal axons, whereas growth cones from nasal retina do not distinguish between nasal and temporal axons.

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Year:  1985        PMID: 4000268     DOI: 10.1038/315409a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  12 in total

Review 1.  Connecting the eye to the brain: the molecular basis of ganglion cell axon guidance.

Authors:  S F Oster; D W Sretavan
Journal:  Br J Ophthalmol       Date:  2003-05       Impact factor: 4.638

2.  Genetic analysis of Drosophila larval optic nerve development.

Authors:  A L Holmes; R N Raper; J S Heilig
Journal:  Genetics       Date:  1998-03       Impact factor: 4.562

Review 3.  A molecular view of vertebrate retinal development.

Authors:  C J Barnstable
Journal:  Mol Neurobiol       Date:  1987 Spring-Summer       Impact factor: 5.590

4.  Retinal axons in Xenopus laevis recognise differences between tectal and diencephalic glial cells in vitro.

Authors:  D J Gooday
Journal:  Cell Tissue Res       Date:  1990-03       Impact factor: 5.249

5.  EphA3 expressed in the chicken tectum stimulates nasal retinal ganglion cell axon growth and is required for retinotectal topographic map formation.

Authors:  Ana Laura Ortalli; Luciano Fiore; Jennifer Di Napoli; Melina Rapacioli; Marcelo Salierno; Roberto Etchenique; Vladimir Flores; Viviana Sanchez; Néstor Gabriel Carri; Gabriel Scicolone
Journal:  PLoS One       Date:  2012-06-07       Impact factor: 3.240

6.  Fluorescent carbocyanine dyes allow living neurons of identified origin to be studied in long-term cultures.

Authors:  M G Honig; R I Hume
Journal:  J Cell Biol       Date:  1986-07       Impact factor: 10.539

7.  Quantitative assessment of computational models for retinotopic map formation.

Authors:  J J Johannes Hjorth; David C Sterratt; Catherine S Cutts; David J Willshaw; Stephen J Eglen
Journal:  Dev Neurobiol       Date:  2014-11-14       Impact factor: 3.964

8.  Computational modeling of retinotopic map development to define contributions of EphA-ephrinA gradients, axon-axon interactions, and patterned activity.

Authors:  Paul A Yates; Alex D Holub; Todd McLaughlin; Terrence J Sejnowski; Dennis D M O'Leary
Journal:  J Neurobiol       Date:  2004-04

9.  Zipper encodes a putative integral membrane protein required for normal axon patterning during Drosophila neurogenesis.

Authors:  D B Zhao; S Côté; F Jähnig; J Haller; H Jäckle
Journal:  EMBO J       Date:  1988-04       Impact factor: 11.598

10.  Membrane glycoproteins involved in neurite fasciculation.

Authors:  F G Rathjen; J M Wolff; R Frank; F Bonhoeffer; U Rutishauser
Journal:  J Cell Biol       Date:  1987-02       Impact factor: 10.539

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